RESUMEN

Frizzled (Fz) signaling regulates cell polarity in both vertebrates and invertebrates. In Drosophila, Fz orients the asymmetric division of the sensory organ precursor cell (pI) along the antero-posterior axis of the notum. Planar polarization involves a remodeling of the apical-basal polarity of the pI cell. The Discs-large (Dlg) and Partner of Inscuteable (Pins) proteins accumulate at the anterior cortex, while Bazooka (Baz) relocalizes to the posterior cortex. Dlg interacts directly with Pins and regulates the localization of Pins and Baz. Pins acts with Fz to localize Baz posteriorly, but Baz is not required to localize Pins anteriorly. Finally, Baz and the Dlg/Pins complex are required for the asymmetric localization of Numb. Thus, the Dlg/Pins complex responds to Fz signaling to establish planar asymmetry in the pI cell.

Asunto(s)

Tipificación del Cuerpo , Proteínas de Ciclo Celular , Polaridad Celular , Proteínas de Drosophila , Drosophila melanogaster/citología , Drosophila melanogaster/embriología , Proteínas de Insectos/metabolismo , Péptidos y Proteínas de Señalización Intracelular , Células Madre/citología , Proteínas Supresoras de Tumor , Animales , Proteínas Portadoras/genética , Proteínas Portadoras/metabolismo , División Celular , Drosophila melanogaster/genética , Drosophila melanogaster/metabolismo , Receptores Frizzled , Inmunohistoquímica , Proteínas de Insectos/genética , Hormonas Juveniles/metabolismo , Sustancias Macromoleculares , Proteínas de la Membrana/fisiología , Modelos Biológicos , Mutación/genética , Neuronas/citología , Neuronas/metabolismo , Pruebas de Precipitina , Unión Proteica , Proteína Quinasa C/metabolismo , Transporte de Proteínas , Receptores Acoplados a Proteínas G , Proteínas Recombinantes de Fusión/metabolismo , Transducción de Señal , Células Madre/metabolismo

RESUMEN

A better understanding of the molecular circuitry in normal ovarian tissues and in ovarian cancer will likely provide new targets for diagnosis and therapy. Recently, much has been learned about the genes expressed in ovarian cancer through studies with cDNA arrays and serial analysis of gene expression. However, these methods do not allow highly quantitative analysis of gene expression on a large number of specimens. Here, we have used quantitative real-time RT-PCR in a panel of 39 microdissected ovarian carcinomas of various subtypes to systematically analyze the expression of 13 genes, many of which were previously identified as up-regulated in a subset of ovarian cancers by serial analyses of gene expression. The genes analyzed are glutathione peroxidase 3 (GPX3), apolipoprotein J/clusterin, insulin-like growth factor-binding protein 2, epithelial cell adhesion molecule/GA733-2, Kop protease inhibitor, matrix gla protein, tissue inhibitor of metalloproteinase 3, folate receptor 1, S100A2, signal transducer and activator of transcription 1, secretory leukocyte protease inhibitor, apolipoprotein E, and ceruloplasmin. All of the genes were found overexpressed, some at extremely high levels, in the vast majority of ovarian carcinomas irrespective of the subtype. Interestingly, GPX3 was found at much higher levels in tumors with clear cell histology and may represent a biomarker for this subtype. Some of the genes studied here may thus represent targets for early detection ovarian cancer. The gene expression patterns were not associated with age at diagnosis, stage, or K-ras mutation status in ovarian cancer. We find that several genes are coordinately regulated in ovarian cancer, likely representing the fact that many genes are activated as part of common signaling pathways or that extensive cross-talk exists between several pathways in ovarian cancer. A statistical analysis shows that genes commonly up-regulated in ovarian cancer may result from the aberrant activation of a limited number of pathways, providing promising targets for novel therapeutic strategies.

Asunto(s)

Regulación Neoplásica de la Expresión Génica , Neoplasias Ováricas/genética , Biomarcadores de Tumor/biosíntesis , Biomarcadores de Tumor/genética , Femenino , Perfilación de la Expresión Génica , Humanos , Análisis de Secuencia por Matrices de Oligonucleótidos , Neoplasias Ováricas/metabolismo , Neoplasias Ováricas/patología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Regulación hacia Arriba

RESUMEN

Difficulties in the detection, diagnosis, and treatment of ovarian cancer result in an overall low survival rate of women with this disease. A better understanding of the pathways involved in ovarian tumorigenesis will likely provide new targets for early and effective intervention. Here, we have used serial analysis of gene expression (SAGE) to generate global gene expression profiles from various ovarian cell lines and tissues, including primary cancers, ovarian surface epithelia cells, and cystadenoma cells. The profiles were used to compare overall patterns of gene expression and to identify differentially expressed genes. We have sequenced a total of 385,000 tags, yielding >56,000 genes expressed in 10 different libraries derived from ovarian tissues. In general, ovarian cancer cell lines showed relatively high levels of similarity to libraries from other cancer cell lines, regardless of the tissue of origin (ovarian or colon), indicating that these lines had lost many of their tissue-specific expression patterns. In contrast, immortalized ovarian surface epithelia and ovarian cystadenoma cells showed much higher similarity to primary ovarian carcinomas than to primary colon carcinomas. Primary tissue specimens therefore appeared to be a better model for gene expression analyses. Using the expression profiles described above and stringent selection criteria, we have identified a number of genes highly differentially expressed between nontransformed ovarian epithelia and ovarian carcinomas. Some of the genes identified are already known to be overexpressed in ovarian cancer, but several represent novel candidates. Many of the genes up-regulated in ovarian cancer represent surface or secreted proteins such as claudin-3 and -4, HE4, mucin-1, epithelial cellular adhesion molecule, and mesothelin. Interestingly, both apolipoprotein E (ApoE) and ApoJ, two proteins involved in lipid homeostasis, are among the genes highly up-regulated in ovarian cancer. Selected serial analysis of gene expression results were further validated through immunohistochemical analysis of ApoJ, claudin-3, claudin-4, and epithelial cellular adhesion molecule in archival material. These experiments provided additional evidence of the relevance of our findings in vivo. The publicly available expression data reported here should stimulate and aid further research in the field of ovarian cancer.

Asunto(s)

Perfilación de la Expresión Génica , Regulación Neoplásica de la Expresión Génica , Neoplasias Ováricas/genética , Transformación Celular Neoplásica/genética , Femenino , Biblioteca de Genes , Humanos , Inmunohistoquímica , Neoplasias Ováricas/metabolismo , Reproducibilidad de los Resultados , Células Tumorales Cultivadas

RESUMEN

BACKGROUND: Membrane-associated guanylate kinases (MAGUKs) assemble ion channels, cell-adhesion molecules and components of second messenger cascades into synapses, and are therefore potentially important for co-ordinating synaptic strength and structure. Here, we have examined the targeting of the Drosophila MAGUK Discs-large (DLG) to larval neuromuscular junctions. RESULTS: During development, DLG was first found associated with the muscle subcortical compartment and plasma membrane, and later was recruited to the postsynaptic membrane. Using a transgenic approach, we studied how mutations in various domains of the DLGprotein affect DLG targeting. Deletion of the HOOK region-the region between the Src homology 3 (SH3) domain and the guanylate-kinase-like (GUK) domain-prevented association of DLG with the subcortical network and rendered the protein largely diffuse. Loss of the first two PDZ domains led to the formation of large clusters throughout the plasma membrane, with scant targeting to the neuromuscular junction. Proper trafficking of DLG missing the GUK domain depended on the presence of endogenous DLG. CONCLUSIONS: Postsynaptic targeting of DLG requires a HOOK-dependent association with extrasynaptic compartments, and interactions mediated by the first two PDZ domains. The GUK domain routes DLG between compartments, possibly by interacting with recently identified cytoskeletal-binding partners.

Asunto(s)

Proteínas de Drosophila , Drosophila/metabolismo , Proteínas de Insectos/metabolismo , Proteínas de la Membrana/metabolismo , Nucleósido-Fosfato Quinasa/metabolismo , Sinapsis/metabolismo , Proteínas Supresoras de Tumor , Animales , Animales Modificados Genéticamente , Membrana Celular/metabolismo , Drosophila/genética , Guanilato-Quinasas , Proteínas de Insectos/química , Proteínas de Insectos/genética , Proteínas de la Membrana/inmunología , Músculos/metabolismo , Unión Neuromuscular , Nucleósido-Fosfato Quinasa/química , Nucleósido-Fosfato Quinasa/genética , Nucleósido-Fosfato Quinasa/inmunología , Estructura Terciaria de Proteína , Transporte de Proteínas , Proteínas Recombinantes de Fusión/inmunología , Proteínas Recombinantes de Fusión/metabolismo , Eliminación de Secuencia/genética

Asunto(s)

Poliposis Adenomatosa del Colon/genética , Neoplasias del Colon/genética , Proteínas del Citoesqueleto/genética , Mutación , Neoplasias Ováricas/genética , Transactivadores , Biomarcadores de Tumor , Transformación Celular Neoplásica , Neoplasias del Colon/patología , Femenino , Mutación del Sistema de Lectura , Humanos , Neoplasias Ováricas/patología , Células Tumorales Cultivadas , beta Catenina

RESUMEN

Discs large (Dlg) was the first identified member of an increasingly important class of proteins called membrane-associated guanylate kinase homologs (MAGUKs), which are often concentrated at cell junctions and contain distinct peptide domains named PDZ1-3, SH3, HOOK, and GUK. Dlg is localized at and required for the formation of both septate junctions in epithelial cells and synaptic junctions in neurons. In the absence of Dlg, epithelia lose their organization and overgrow. We tested the functions of each domain of Dlg in vivo by constructing transgenic flies expressing altered forms of the protein. In the first set of experiments each domain was examined for its ability to correctly target an epitope-tagged Dlg to pre-existing septate junctions. Based on these results the Hook domain is necessary for localization of the protein to the cell membrane and the PDZ2 is required for restricting the protein to the septate junction. In the second set of experiments each domain was tested for its role in growth regulation and organization of epithelial structure. These results show that PDZ1 and GUK are apparently dispensable for function, PDZ2 and PDZ3 are required for growth regulation but not for epithelial structure, and SH3 and HOOK are essential for both aspects of function. The results demonstrate the functional modularity of Dlg and clarify the functions of individual MAGUK domains in regulating the structure and growth of epithelial tissue.

Asunto(s)

Proteínas de Drosophila , Drosophila/fisiología , Proteínas de Insectos/fisiología , Proteínas de la Membrana/fisiología , Nucleósido-Fosfato Quinasa/fisiología , Proteínas Supresoras de Tumor , Animales , Animales Modificados Genéticamente , Sitios de Unión , Transporte Biológico , Mapeo Cromosómico , Drosophila/genética , Drosophila/crecimiento & desarrollo , Femenino , Guanilato-Quinasas , Proteínas de Insectos/genética , Masculino , Proteínas de la Membrana/genética , Nucleósido-Fosfato Quinasa/genética , Fenotipo , Eliminación de Secuencia , Relación Estructura-Actividad

RESUMEN

5-Enolpyruvylshikimate-3-phosphate (EPSP) synthase, the product of the Escherichia coli aroA gene, has been overproduced in E. coli BL21(lambda DE3) under the control of the T7 gene 10 promoter and ribosome binding site, to a level of approximately 50% of total cell protein. EPSP synthase is the primary target of the post-emergence herbicide, glyphosate, commonly known as Roundup. A simple two step purification is described, which results in 99% pure homogeneous protein (as determined by PAGE). The integrity of the protein has been compared with previously characterized protein from E. coli AB2829(pKD501) by determination of its kinetic parameters, N-terminal protein and DNA sequences, amino acid analysis and 13C-NMR spectroscopy. This new overproducing strain readily provides the gram quantities of highly pure protein required for NMR studies of the active site and the development of novel time-resolved solid-state NMR techniques currently underway in this laboratory.

Asunto(s)

Transferasas Alquil y Aril , ARN Polimerasas Dirigidas por ADN/genética , Escherichia coli/enzimología , Regiones Promotoras Genéticas , Proteínas Recombinantes/biosíntesis , Fagos T/genética , Transferasas/biosíntesis , 3-Fosfoshikimato 1-Carboxiviniltransferasa , Secuencia de Bases , Escherichia coli/genética , Vectores Genéticos , Cinética , Datos de Secuencia Molecular , Mutagénesis Sitio-Dirigida , Proteínas Recombinantes/genética , Proteínas Recombinantes/aislamiento & purificación , Transferasas/genética , Transferasas/aislamiento & purificación